A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265169



Internal ID20474387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42813988..42813988hg38UCSC Ensembl
chr5:42814090..42814090hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766430
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265169
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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